STRUCTURAL AND FUNCTIONAL-STUDIES ON THE HUMAN HEPATIC INTERLEUKIN-6 RECEPTOR - MOLECULAR-CLONING AND OVEREXPRESSION IN HEPG2 CELLS

被引:49
作者
SCHOOLTINK, H
STOYAN, T
LENZ, D
SCHMITZ, H
HIRANO, T
KISHIMOTO, T
HEINRICH, PC
ROSEJOHN, S
机构
[1] RHEIN WESTFAL TH AACHEN,INST BIOCHEM,PAUWELSTR 30,W-5100 AACHEN,GERMANY
[2] OSAKA UNIV,INST MOLEC & CELLULAR BIOL,OSAKA,JAPAN
关键词
D O I
10.1042/bj2770659
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
cDNAs coding for the human hepatic interleukin-6 receptor (IL-6-R) have been isolated from a library made from poly(A) RNA of dexamethasone-treated human hepatoma cells (HepG2). We found the hepatic IL-6-R to be identical to the one expressed by leucocytes. A polyclonal antiserum was raised in rabbits against the IL-6-R protein expressed in Escherichia coli. Although the entire IL-6-R protein was used for immunization, only antibodies to the cytoplasmic domain of the IL-6-R were obtained. It is demonstrated by affinity cross-linking and subsequent immunoprecipitation with antibodies against the ligand as well as against the receptor that the cloned cDNA codes for the functional IL-6-R on HepG2 cells. When the hepatic IL-6-R cDNA was overexpressed in HepG2 cells, these cells became more sensitive to low concentrations of IL-6 with respect to the induction of gamma-fibrinogen mRNA.
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页码:659 / 664
页数:6
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